Llwytho...

inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing

The detection of copy number variations (CNVs) on whole-exome sequencing (WES) represents a cost-effective technique for the study of genetic variants. This approach, however, has encountered an obstacle with high false-positive rates due to biases from exome sequencing capture kits and GC contents....

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Evol Bioinform Online
Prif Awduron: Chanwigoon, Saowwapark, Piwluang, Sakkayaphab, Wichadakul, Duangdao
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: SAGE Publications 2020
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7520931/
https://ncbi.nlm.nih.gov/pubmed/33029071
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1176934320956577
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!